Risk Management Masterclass [2024] | Certification Course

Be an expert in ISO 14971 (RM) and ISO 13485 (QMS). Create risk assessment docs like DFMEA, HAZOP, HACCP from scratch

3.74 (92 reviews)
Udemy
platform
English
language
Management
category
Risk Management Masterclass [2024] | Certification Course
3,014
students
6 hours
content
May 2023
last update
$79.99
regular price

What you will learn

Become an expert in creating Risk Management documents from scratch, such as PFMEA, DFMEA, HAZOP, HACCP for any enterprise.

Learn-depth on how to perform Risk Assessment, Risk Evaluation, Risk Measurement, Risk Control and Benefit-Risk Analysis!

In-depth understanding of Regulatory standards for GMP environment such as ISO 14791:2019, EU 2017/745 MDR, 21 CFR 820, SOR/98-282, ISO13485 and ISO 22000

Be proficient in what Food and Drug Administration (FDA) auditors are looking for while doing Quality audits in medical device and food industry,

Learn why CAPA, Non conformances, IQ/OQ/PQ, complaint handling process are crucial for medical device industry

Learn in-depth about Quality Management system (QMS) regulations from different countries around the world

How Risk management Activities is essential in creating a good manufacturing practice (GMP) environment.

Why take this course?

  • The most extensive course on Risk Management available in Udemy!

  • This course is designed to teach you everything that you need to know to become a Subject Matter Expert (SME) in Risk Management  and Quality Management System (QMS) within Medical device, pharmaceutical industry and any other enterprise that conducts risk management activity.

  • Regardless of your current skills and experience, after taking this course, you will be comfortable communicating to experts in medical device industry about Quality management systems (QMS) and risk management (RM) standards and regulations.

  • By the end of this course you will be a pro at creating complex Risk Assessment and Risk Measurement documents such as PFMEA, DFMEA, HACCP, HAZOP, Benefit-Risk Analysis, Post Market Surveillance Report (PMSR), Clinical Effects Analysis Report (CEA) from the scratch! Knowing this skills will set you apart from the crowd and you can easily land you six-figure jobs in a reputed medical device companies.

  • You will be well versed in rules, regulations and standards for medical device industries across the world such as ISO14971 (Risk Management, ISO) , ISO13485, ISO 22000,  21CFR810 (FDA, USA), RDC 40/2015 (Anvisa, Brazil), EU 2017/745 MDR, MHLW MO 169 (PMDA, Japan) and TGR 2002 (TGA, Austrialia) and be able to talk about them in meetings, interviews and even with auditors.

  • You will learn how processes like complaint reviews, Corrective and Preventative Maintenance (CAPA), Process Validation (PV), Equipment Qualification (IQ/OQ/PQ) ties into Risk Management and why companies need to do these activities.

  • Whether you are just getting into Risk Management, or wants to freshen up your skills, or are looking to advance your career in the field, this course can provide you with more than enough knowledge to be the top 5% in your organization.


    1. Note: This course is directly related to and applies to Enterprise Risk Management (ERM). Medical device and Pharmaceutical companies are an enterprises themselves so this course teaches you everything you need to know to manage risks in an enterprise.  In fact, you will learn risk management in so much in-depth from this course that you can tackle risk management activities on any enterprise.

    2. Note: This course also ties into Financial Risk Management (FRM) as we go in depth on the types of risks companies deals with, and financial risk is one of them. Hence students wanting to learn FRM can also greatly benefit from this course.

Screenshots

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Reviews

Luca
January 18, 2024
too generic, even for introduction. slides at the end of long speech are too fast in first chapter. Proceeding is the same, generic and not in depth. It's more a chat with a friend about some topic than a training.
Natalia
January 15, 2024
Thanks for good lectures! Easy and basic to understanding all of the course information. Good links on the regulatory documentation and whole diving to course!
Rajesh
November 25, 2023
The contents are of very basic level. The relevant definitions shall be from the regulatory guidelines and not based upon individual's concept understanding
Fabio
October 25, 2023
I was expecting something more substantial, with more examples and not that superficial, for the price is informative, but still, I have seen better courses for the same price
Urvi
July 12, 2023
Amazing content to do for expanding your Risk management area. Liked the live demo for each document looks like for FMEA, PFMEA, HAZOP file, and HACCP plan.
Anna
July 7, 2023
Very poor quality and super superficial. The author just opens the documents from the internet and quickly scrolls through them. Constantly advising to learn from the docs rather than people and online courses. Then what's the point of creating your online course? Moreover, the author can't even explain what is a medical device and how it's different from pharmaceuticals! Almost no examples. A few examples provided are about food and have nothing to do with medical devices.
Anna
July 7, 2023
The TV was on on some of the slides with the background notise being very disturbing when trying to listen and concentrate on what the guy was saying in the video!
Arunprasath
June 23, 2023
Thanks for the good session. it would be greater if we could get some examples like Scenarios & solutions for RM with respect to medical devices.
Sharon
April 11, 2023
The instructor goes in depth and covers a wide range of risk management activities. Would recommend! He's also easy to get a hold of for questions!

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4686646
udemy ID
5/14/2022
course created date
4/11/2023
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